Showing 1 to 2 of 2 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000212.3(ITGB3):c.197T>G (p.Leu66Arg) | Benign | Glanzmann thrombasthenia | 2023-12-19 | 2.0 | ClinGen Platelet Disorders Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines Version 2.1 | ITGB3 |
| View | NM_000212.3(ITGB3):c.197T>G (p.Leu66Arg) | Uncertain Significance | Glanzmann's thrombasthenia | 2021-08-20 | 1.0 | - | ITGB3 |
Showing 1 to 2 of 2 rows